| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:47356664-47356887 | Rare:51 | ||||
| chr20:47501711-47502016 | Common:1; Rare:108 | ||||
| chr20:47786469-47786797 | Common:7; Rare:58 | ||||
| chr20:49046115-49046401 | Common:3; Rare:88 | ||||
| chr20:49219281-49219541 | Rare:118 | ||||
| chr20:49278036-49278291 | Rare:71 | ||||
| chr20:49278425-49278704 | Common:10; Rare:111 | ||||
| chr20:49812765-49812925 | Common:2; Rare:44 | ||||
| chr20:49915496-49915556 | Common:1; Rare:18 | ||||
| chr20:49936246-49936415 | Rare:66 | ||||
| chr20:50113121-50113259 | Common:5; Rare:64 | ||||
| chr20:50115935-50116087 | Common:2; Rare:36 | ||||
| chr20:50153651-50153933 | Common:2; Rare:115 | ||||
| chr20:50510109-50510428 | Common:3; Rare:128 | ||||
| chr20:50958454-50958851 | Common:1; Rare:146; Clinvar:4; Clinvar (benign):4 |